Porous nanostructured polyimide networks and methods of manufacture

ABSTRACT

Porous three-dimensional networks of polyimide and porous three-dimensional networks of carbon and methods of their manufacture are described. For example, polyimide aerogels are prepared by mixing a dianhydride and a diisocyanate in a solvent comprising a pyrrolidone and acetonitrile at room temperature to form a sol-gel material and supercritically drying the sol-gel material to form the polyimide aerogel. Porous three-dimensional polyimide networks, such as polyimide aerogels, may also exhibit a fibrous morphology. Having a porous three-dimensional polyimide network undergo an additional step of pyrolysis may result in the three dimensional network being converted to a purely carbon skeleton, yielding a porous three-dimensional carbon network. The carbon network, having been derived from a fibrous polyimide network, may also exhibit a fibrous morphology.

RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No.15/654,111, filed Jul. 19, 2017, which is a continuation of U.S.application Ser. No. 14/261,399, filed Apr. 24, 2014, which is acontinuation of U.S. application Ser. No. 13/214,633, filed Aug. 22,2011, which claims priority to U.S. Provisional Patent Application Ser.No. 61/375,656, filed Aug. 20, 2010, each of which is incorporatedherein by reference in its entirety for all purposes.

FEDERALLY SPONSORED RESEARCH

Research leading to various aspects of embodiments presented herein weresponsored, at least in part, by the National Science Foundation, GrantNo. CHE-0809562 and Grant No. CMMI-0653919. The United States Governmentmay have certain rights in the invention.

BACKGROUND 1. Field

Aspects herein relate to nanostructured polyimide networks, carbonizedderivatives, related materials, uses thereof, and methods ofmanufacture.

2. Discussion of Related Art

Three-dimensional porous architectures are a desirable form factor formany materials as they allow installation of new properties into amaterial not possessed by the non-porous form of a material. Porousarchitectures possessing nanostructured features, such as nanopores ornanoparticulate solid frameworks, are further desirable in many cases asthey can possess new and/or more extreme properties than porousarchitectures without nanostructured features.

Aerogels are an example of a porous architecture possessingnanostructured features. Aerogels are materials comprised ofthree-dimensional assemblies of nanoparticles or nanostructures thatexhibit high materials and ultra-low densities Aerogel materials aretypically produced by forming a gel that includes a porous solidcomponent and a liquid component and then removing the liquid componentby supercritically, subcritically, or freeze drying the wet gel toisolate the porous solid component. This porous solid component is anaerogel. Supercritical drying involves the liquid being transformed intoa fluid above its critical point and removing the fluid while leavingthe porous solid structure generally intact. Subcritical drying involvesevaporation of the liquid below its critical point in a way that leavesthe porous solid structure generally intact. Freeze drying involvesfreezing of the liquid component and sublimation of the resulting solidin a way that leaves the porous solid structure generally intact.

The large internal void space in aerogels and other nanostructured andnon-nanostructured three-dimensional porous networks generally providesfor a low dielectric constant, a low thermal conductivity, and a highacoustic impedance. These materials have been considered for a number ofapplications including thermal insulation, lightweight structures, andimpact resistance.

SUMMARY

Articles and methods for manufacturing three-dimensional porouspolyimide networks and three-dimensional porous carbon networks aredescribed.

Three-dimensional porous polyimide networks can be prepared by mixing adianhydride and a diisocyanate in a solvent comprising a pyrrolidone andacetonitrile at room temperature to form a sol-gel material andsubsequently drying the sol-gel material to form a polyimide aerogel.Drying may be performed supercritically, subcritically, or by freezedrying. In some embodiments, a polyimide aerogel manufactured by methodsdescribed herein may have a fibrous morphology which may or may not alsoinclude particulate features.

Three-dimensional porous carbon network aerogels may also bemanufactured from polyimide aerogels through a conversion step. Once apolyimide aerogel is formed, the aerogel may be subjected to a pyrolysisstep, giving rise to a carbon skeleton in the aerogel, hence, a carbonaerogel. In some embodiments, a polyimide aerogel having a fibrousmorphology that is subject to the pyrolysis step may give rise to acarbon aerogel also having a fibrous morphology.

In some cases, three-dimensional porous polyimide networks notconsidered aerogels may be produced. Likewise, three-dimensional porouscarbon networks not considered aerogels may be derived from suchthree-dimensional polyimide networks.

Various embodiments of the present invention provide certain advantages.Not all embodiments of the invention share the same advantages and thosethat do may not share them under all circumstances.

Further features and advantages of the present invention, as well as thestructure of various embodiments of the present invention are describedin detail below with reference to the accompanying drawings.

BRIEF DESCRIPTION OF DRAWINGS

The accompanying drawings are not intended to be drawn to scale. Forpurposes of clarity, not every component may be labeled in everydrawing. Various embodiments of the invention are described, by way ofexample, in the accompanying drawings. In the drawings:

FIG. 1 depicts chemical structures for PMDA, MDI and MDA;

FIG. 2a shows a flow chart for the preparation of a three-dimensionalporous polyimide network in accordance with some embodiments;

FIG. 2b shows another flow chart for the preparation of athree-dimensional porous polyimide network in accordance with someembodiments;

FIG. 3a depicts a flow chart for the preparation of a three-dimensionalporous polyimide network in accordance with some embodiments;

FIG. 3b shows another flow chart for the preparation of athree-dimensional porous polyimide network in accordance with someembodiments;

FIG. 3c shows yet another flow chart for the preparation of athree-dimensional porous polyimide network in accordance with someembodiments;

FIG. 4 illustrates a reaction step in forming a three-dimensional porouspolyimide network in accordance with some embodiments;

FIG. 5a depicts reactions where a polyimide is formed through isocyanateand amine routes in accordance with some embodiments;

FIG. 5b depicts more reactions where a polyimide is formed throughisocyanate and amine routes in accordance with some embodiments;

FIG. 6a depicts a molecular structure of a three-dimensional porouspolyimide network formed through an amine route;

FIG. 6b illustrates a molecular structure of a three-dimensional porouspolyimide network formed through an isocyanate route in accordance withsome embodiments;

FIG. 7 shows a nuclear magnetic resonance (NMR) spectra of a PMDA/MDImixture in accordance with some embodiments;

FIG. 8 illustrates photographs of polyimide aerogels synthesized inaccordance with some embodiments;

FIG. 9 depicts an infrared (IR) spectra of polyimide aerogels preparedin accordance with some embodiments;

FIG. 10 illustrates a NMR spectra of polyimide aerogels prepared inaccordance with some embodiments;

FIG. 11 depicts a shrinkage data for polyimide aerogels prepared inaccordance with some embodiments;

FIG. 12 shows nitrogen sorption data for polyimide aerogels prepared inaccordance with some embodiments;

FIG. 13 shows scanning electron microscope (SEM) images of polyimideaerogels prepared in accordance with some embodiments;

FIG. 14 shows more SEM images of polyimide aerogels prepared inaccordance with some embodiments;

FIG. 15 depicts small angle neutron scattering data of polyimideaerogels prepared in accordance with some embodiments;

FIG. 16 illustrates a compressive stress-strain curve of polyimideaerogels prepared in accordance with some embodiments;

FIG. 17 shows thermogravimetric analysis (TGA) data of polyimideaerogels prepared in accordance with some embodiments;

FIG. 18 shows Raman spectra polyimide aerogels prepared in accordancewith some embodiments;

FIG. 19 shows SEM images and nitrogen sorption data for carbon aerogelsprepared in accordance with some embodiments; and

FIG. 20 shows more SEM images and nitrogen sorption data for carbonaerogels prepared in accordance with some embodiments.

DETAILED DESCRIPTION

Porous three-dimensional networks of polyimide and porousthree-dimensional networks of carbon and methods of their manufactureare described herein. In some embodiments, three-dimensional porouspolyimide networks (e.g., aerogels) are prepared by mixing a dianhydrideand a diisocyanate in a solvent comprising a pyrrolidone and anacetonitrile at room temperature to form a sol-gel material. The sol-gelmaterial may be dried supercritically or subcritically so as to form thethree-dimensional porous polyimide network. The three-dimensional porouspolyimide network may also exhibit a fibrous morphology. In someembodiments, the three-dimensional porous polyimide network may besubject to an additional step of pyrolysis resulting in the threedimensional network of polyimide being converted to a carbon skeleton,yielding a three-dimensional porous carbon network. Thethree-dimensional porous carbon network, having been derived from afibrous three-dimensional porous polyimide network, may also exhibit afibrous morphology.

Three-dimensional porous polyimide networks may be prepared via aone-step room-temperature synthesis route involving reaction of adianhydride with a diisocyanate. Using an isocyanate to form thepolyimide network using methods described herein provides certainadvantages: a) CO₂ is the only substantial byproduct; b) sacrificialdehydrating agents (e.g., acetic anhydride/pyridine) are not requiredfor gelation; c) gelation and imidization take place at room temperatureand, thus, post-gelation curing at high temperatures (e.g., 190° C.) inorder to complete imidization is not required; d) use of isocyanates ischeaper than use of amines from the traditional route; e) higher densitybifunctional aerogels for dual-purpose applications (e.g. thermalinsulators that are also used as structural components; impact dampeningmaterials that are also used as structural components) are easilyaccessible with no solubility issues in turn extending the accessibledensity range upwards, while the polyamic acid route encounterssolubility issues at higher concentration sols; and f) an entangledfiber nanomorphology stabilizes the nanostructure, extending theaccessible density range downwards.

Three-dimensional porous polyimide networks such as polyimide aerogelsmay be manufactured using a route that involves condensation of adianhydride and a diamine to form a polyamic acid solution that isdehydrated with an anhydride to form polyimide. In some cases, use of asacrificial dehydration step is generally expensive with respect to thecost of materials and removal of the byproducts. A further complicationmay be the kinetic formation of isoimides which can be converted to morethermodynamically stable imides by high-temperature treatment. Toaccommodate this, the dehydration step may be carried out at elevatedtemperatures directly (>130° C.). Preparation of certain polyimideaerogels are described in U.S. Pat. No. 7,074,880 entitled “Polyimideaerogels, carbon aerogels, and metal carbide aerogels and methods ofmaking same” and is incorporated herein by reference in its entirety.

Polyimide aerogels synthesized via a conventional route using diamine(PI-AMN) as compared to routes contemplated by the inventors anddescribed herein using isocyanate (PI-ISO) may have similar surfaceareas (e.g., for 20% solid formulation PI-ISO: 351 m²/g, density=0.196g/cm³; PI-AMN: 377 m²/g, density=0.291 g/cm³). However, thenanomorphologies of polyimide aerogels prepared using isocyanate may becompletely different from nanomorphologies of polyimide aerogelsprepared using diamine. For example, for a similar chemical composition,PI-ISO may have a fibrous morphology, while PI-AMN have a particulatemorphology. In general, PI-ISO may also be more robust and may shrinkless compared to PI-AMN. Upon pyrolysis, polyimide aerogels can beconverted to carbon aerogels which may retain the main morphologicalcharacteristics (fibrous versus particulate) of their parent polyimideaerogels.

Three-dimensional porous polyimide networks such as polyimide aerogelssynthesized through the isocyanate route are less prone to shrinkageduring processing compared to polyimide aerogels synthesized through thediamine route; densities as low as 0.04 g/cm³ have been obtained.Further, owing to solubility issues, PI-AMN aerogels generally cannot bemade with sols above 20% w/w solids in the sol. Resulting PI-AMNaerogels had a density of 0.291 g/cm³. However, more concentrated solsare possible via the isocyanate route. For example, PI-ISO aerogels fromsols with 30% w/w solids had a density of about 0.304 g/cm³. Uponcarbonization at 800° C., PI-ISO retain their parent nanomorphology,which may be fibrous. The ability to prepare higher density polyimideaerogels and other three-dimensional porous polyimide networks extendsthe range of compressive strength and stiffness attainable for polyimidenetworks and their carbonized derivatives.

Three-dimensional porous polyimide networks such as polyimide aerogelsprepared in accordance with methods described herein may exhibit asuitable degree of shrinkage. In some embodiments, three-dimensionalporous polyimide networks (e.g., polyimide aerogels) prepared withisocyanate may exhibit a shrinkage of less than 30%, less than 20%, lessthan 10%, less than 5%, less than 2%, less than 1%. In some cases, theshrinkage of a polyimide aerogel may be affected by the percent solidsw/w. For example, when the percentage of solids in the sol is lower, thedegree of shrinkage for the polyimide aerogel may be greater.

The density of three-dimensional porous polyimide networks orthree-dimensional porous carbon networks prepared from pyrolysis ofpolyimide networks using methods described herein may be between, forexample, about 1 mg/cc and about 550 mg/cc, or between about 100 mg/ccand about 400 mg/cc. In some embodiments, the density ofthree-dimensional porous polyimide networks or three-dimensional porouscarbon networks prepared from pyrolysis of polyimide networks may begreater than about 300 mg/cc.

Aerogels described herein may include a three-dimensional porous networkof secondary particles and primary particles. Porous secondary particleshaving a diameter of between about 5-10 nm are made up of nonporousprimary particles having a diameter of less than about 1 nm. While theprimary particles are arranged in a manner that forms micropores withinthe secondary particles, larger mesopores arise through the arrangementof secondary particles relative to one another. A silica nanoparticlenetwork in the form of an aerogel may include mesopores having voidsthat are between 2-50 nm in diameter between secondary particles.Primary particles include voids that are less than 2 nm in diameter.

Three-dimensional porous networks discussed herein may have fibrousmorphologies where the networks may include nanofibers having variousdiameters and lengths. In some embodiments, fibrous morphologies of suchnetworks include fibers having an average diameter ranging between about1 nm and about 500 nm (e.g., between about 10 nm and about 400 nm,between about 100 nm and about 300 nm) or less than 500 nm (e.g., lessthan 400 nm, less than 300 nm, less than 200 nm). In some embodiments,fibrous morphologies of porous networks described herein include fibershaving an average length of at least 50 nm and may extend into themicron length scale. The average aspect ratio of fibers in athree-dimensional porous networks having a fibrous morphology, such asan aerogel may be greater than 2, greater than 5, greater than 10,greater than 20, greater than 50, etc. Three-dimensional porous networksdescribed herein that exhibit a fibrous morphology may include bothfibrous and non-fibrous features (e.g., particulate), but, in someembodiments, could also contain only fibrous features, free ofnon-fibrous features.

Any appropriate isocyanate, such as a diisocyanate or triisocyanate, maybe used for forming a sol-gel material to produce a three-dimensionalporous polyimide network, such as a polyimide aerogel. For example,suitable non-limiting diisocyanates may include4,4′-diisocyanatodiphenylmethane or methylene di-p-phenyldiisocyanate(MDI).

Any appropriate dianhydride may be used to react with an isocyanate(e.g., diisocyanate, triisocyanate) in forming a sol-gel material toproduce a three-dimensional porous polyimide network, for example, apolyimide aerogel. In an embodiment, a suitable non-limiting dianhydrideincludes pyromellitic dianhydride (PMDA).

A suitable solvent may be used along with the isocyanate and thedianhydride. In various embodiments, a pyrrolidone (e.g.,N-methyl-2-pyrrolidone, NMP), acetonitrile, acrylonitrile, acetone,and/or combinations thereof may be used to form a three-dimensionalporous polyimide network, such as a polyimide aerogel.

In some embodiments, monolithic polyimide aerogels (PI-ISO) may beprepared by drying wet gels synthesized via a rather underutilizedroom-temperature reaction of pyromellitic dianhydride (PMDA) with4,4′-methylene di-p-phenyldiisocyanate (MDI). The reaction may beobserved using liquid-phase ¹³C-NMR in DMSO-d₆ which, for some cases,has indicated that the reaction proceeds through a seven-member ringintermediate that collapses to the imide by expelling CO₂. PI-ISO may becharacterized and compared with aerogels obtained via the classicreaction of PMDA and 4,4′-methylenedianiline (MDA), referred to asPI-AMN. The two materials, PI-ISO and PI-AMN may be chemicallyidentical, showing similar degrees of crystallinity (30-45%, by XRD),and both including similarly sized primary particles (6.1-7.5 nm,verified by SANS). For some embodiments, they both may contain meso- andmacroporosity by N₂-sorption porosimetry and may exhibit similar BETsurface areas (300-400 m² g⁻¹).

A major difference between PI-AMN and PI-ISO prepared using methodsdescribed herein, however, is that PI-AMN are particulate while PI-ISOmay be fibrous in morphology. Without being limited to any oneparticular mechanism, the difference in morphology may be due to therigidity of the seven-member ring intermediate of PI-ISO. PI-AMN shrinkssignificantly during processing (up to 40% in linear dimensions), butcan exhibit stronger mechanical properties than PI-ISO of the samedensity. Upon pyrolysis at 800° C., both PI-ISO and PI-AMN have beenobserved to convert to porous carbons. PI-AMN lose their nanomorphologyand more than ⅔ of their surface area, as opposed to PI-ISO, whichretains their nanomorphology and surface area. Etching with CO₂ at 1000°C. increases the surface area of both PI-AMN and PI-ISO, and improvesthe electrical conductivity of the latter. In one embodiment, etchingresulted in an increase of surface area in PI-AMN to 417 m²/g and anincrease in PI-ISO to 1010 m²/g and an increase in electricalconductivity in PI-ISO by a factor of 70. Etching for longer periods oftimes, with higher flow rates of CO₂, and higher temperatures canfurther increase these values.

Among engineering plastics, polyimides demonstrate good chemicalresistance as well as excellent mechanical properties and stability athigh temperatures. For example, a special formulation referred to asPMR-15 is emerging as an aerospace industry standard for replacing metalcomponents in jet engines and is rated at 290° C. for 10,000 h. In thatregard, polyimide aerogels could be ideal materials for high-temperaturelow-k dielectrics for fast electronics (where k stands for thedielectric constant), and for high-temperature thermal insulation withadvantages over blown closed-cell macroporous polyimide foams already inuse for that purpose. As mentioned, polyimide aerogels may besynthesized employing a conventional two-step DuPont route utilizingdianhydrides and diamines. The two monomers react at room temperatureyielding a polyamic acid solution that subsequently is dehydrated to thepolyimide with acetic anhydride and a base-catalyst (e.g., pyridine ortriethylamine). A post-gelation high-temperature treatment of wet gelsensures complete imidization and conversion of undesirable isoimides toimides. Though chemical dehydration of the polyamic acid isenergy-intensive and introduces by-products, industrially, dehydrationand imidization are carried out by direct heating of the polyamic acidat high temperatures (˜200° C.). In an attempt to adapt this directheating method for the synthesis of aerogels, however, precipitates wereobtained rather than gels.

Polyimide aerogels described herein may also be synthesized via aone-step room-temperature route that involves reaction of anhydrideswith isocyanates. In some embodiments, pyromellitic dianhydride (PMDA)is reacted with 4,4′-methylene diphenyl diisocyanate (MDI). Forcontrast, a route involving the reaction of PMDA with4,4′-methylenedianiline (MDA) will be considered. Resulting aerogelsfrom both routes are chemically identical (by IR and solids CPMAS¹³C-NMR). However, despite similar degrees of crystallinity and primaryparticle sizes (by XRD and SANS, respectively), their nanomorphology (bySEM) may be quite different: polyimides from the amine route (PI-AMN)are particulate, while those from the isocyanate route (PI-ISO) arefibrous. One of ordinary skill in the art would be able to recognize thedifference between a particulate and fibrous morphology. Upon pyrolysis,both kinds of polyimide aerogels may be converted to carbon aerogels,which, in the case of PI-ISO retain the fibrous morphology of theirparent polyimides.

EXAMPLES Synthesis of PI-ISO Versus PI-AMN

FIG. 1 illustrates the chemical structures for a number of polyimideaerogel precursors, namely PMDA, MDI and MDA. FIGS. 2a-2c and 3a-3bsummarize various embodiments of the synthesis of PI-AMN and PI-ISOaerogels. Typical samples processed under the different conditionsdiscussed below are shown in the figures.

PI-AMN were prepared through a polyamic acid step (see FIGS. 5a and 5b )according to a modification of the Aspen Aerogels adaptation of theclassic DuPont route. According to the latter, typically polyamic acidis not isolated from its preparation solution (inN-methyl-2-pyrrolidone, NMP) and is dehydrated either thermally (>190°C.) or chemically at room temperature with acetic anhydride/base (e.g.,pyridine, triethylamine, etc.). At first, to improve the Aspen Aerogelsprotocol that opts for chemical dehydration, bypassing the latter stepby direct heating of NMP solutions of the polyamic acid may beperformed, yet may result in precipitation rather than gelation. Thus,room-temperature (RT) chemical dehydration was used with aceticanhydride/pyridine. The bulk density of the final aerogels may be variedby successive dilutions of the polyamic acid solution before adding thedehydrating agents. Although addition of the dehydrating agents into thepolyamic acid solution induces gelation, in general polyimides obtainedby that route required heating at elevated temperatures in order tocomplete imidization and to convert any kinetically formed isoimides tothermodynamically more stable imides.

Room-temperature PI-AMN gels were solvent-exchanged with ethanol anddried to aerogels (abbreviated as PI-AMN-RT) using liquid CO₂ extractedsupercritically. Subcritical drying of the aerogels may also beperformed. According to IR, PI-AMN-RT aerogels do not contain detectableamounts of isoimide (with expected absorption at 1800 cm⁻¹), but theabsorption at ˜3500 cm⁻¹ indicates that they may contain amides andtherefore unreacted polyamic acid. Heating PI-AMN-RT aerogels at 190° C.causes extensive shrinkage and results into xerogel-like materials witha loss in surface area. Hence, PI-AMN was heated in a solvent-swollenstate, and thus imidization was completed before drying by transferringwet gels into NMP followed by heating at 190° C. Subsequently, wet gelsmay be cooled to RT, NMP was exchanged with ethanol, and ethanol-filledwet-gels may be supercritically dried with CO₂ yielding PI-AMN-190aerogels. In some cases, even though absorption at ˜3500 cm⁻¹ decreases,it did not disappear. Further, even by heating in the solvent-swollenstate, PI-AMN samples shrink significantly relative to their molds (upto 40% in linear dimensions) irrespective of their bulk density;shrinkage is not caused by the heat treatment at 190° C., as aerogelsamples either dried directly after gelation (PI-AMN-RT) or afterheating at 190° C. in NMP according to FIGS. 2a and 3a (PI-AMN-190) aresimilar in size. Rather, shrinkage of PI-AMN samples may be attributedto the innate chemistry of the gel-forming process.

On the other hand, PMDA/MDI solutions gel directly at room temperaturewithout use of additional reagents. The reaction was followed up to thegelation point using liquid-phase ¹³C-NMR in DMSO-d₆. As shown in FIGS.5a and 5b , it can be seen that the reaction proceeds through aseven-member ring intermediate which collapses to the imide by expellingCO₂. At the gelation point (˜7.5 h), a significant amount of theseven-member ring intermediate remains and still reacts. On the otherhand, the reaction may proceed much slower in NMP at RT and gelation maytake up to 48 h depending on the monomer concentration. Gelation may becarried out at RT in DMSO. Although PI aerogels are opaque, their wetgel precursors are generally translucent allowing visual inspection oftheir interior. It can be seen that PI-ISO aerogels obtained from DMSOsols at RT may contain large bubbles (CO₂) entrapped in their bulk.

In some embodiments, the seven-member intermediate may be considered anin-situ foaming agent leading to foam-like PI-ISO architectures definedby porous walls. Macroscopically void-free (i.e., bubble-free) PI-ISOaerogel monoliths were obtained by two methods (shown in FIGS. 2b, 3b-3c): either, (a) by RT gelation of PMDA/MDI in mixtures of NMP with DMSOor acetonitrile (samples referred to as PI-ISO-RT); or, (b) by gelationin pure NMP at slightly elevated temperatures by stepwise heating from60° C. to 90° C. (see FIGS. 2b, 3b-3c , samples referred to asPI-ISO-90). It can be appreciated that other heating arrangements may bepossible. The first method combines sufficiently low-viscosity sols withaffordable gelation times (30-33 h for the 15% w/w solids formulation)allowing CO₂ to be dissipated and bubble formation to be avoided. Thesecond method has the advantage of comparing PI-ISO and PI-AMN preparedin environments of similar polarity (both in NMP); step-wise heating ofthe PMDA/MDI sol in NMP ensured defect-free monoliths, while directheating at 90° C. led to foams qualitatively similar to those obtainedin DMSO at RT (i.e., with bubbles). All gels were aged ˜4× theirgelation time in their molds, were solvent-exchanged with ethanol, andsupercritically dried with CO₂.

IR spectra of PI-ISO-RT look essentially identical to IR spectra ofPI-AMN-190, but the solid-state ¹³C-NMR spectra of the two materialsshow differences in the relative peak intensities which are attributedto differences in polymer length and therefore to the polarity of thesol (as a reminder, PI-ISO-RT were prepared in NMP/acetonitrile orNMP/DMSO mixtures, while PI-AMN-190 were prepared in pure NMP). FIG. 9shows IR spectra of polyimide aerogel samples where peak assignmentsinclude: a, b (1777 cm⁻¹ and 1723 cm⁻¹) asymmetric and symmetricstretching vibrations of C═O; c (1511 cm⁻¹) aromatic ring breathingmodes; d (1366 cm⁻¹) C—N—C imide ring stretching; e, f (1123 cm⁻¹ and780 cm⁻¹) imide ring vibrations; and g (723 cm⁻¹) imide ring bending.

FIG. 10 shows solids CPMAS ¹³C-NMR of samples as indicated. Samplesshown are prepared using the 15% solids formulation (Table 1) withPI-AMN and PI-ISO-90 prepared in NMP; and PI-ISO-RT prepared inNMP/CH₃CN (3:1 w/w). Notably, the peak in the ¹³C-NMR spectrum ofPI-AMN-190 at 142 ppm (carbon number 16, see FIGS. 5a and 5b ) appearsonly as a shoulder in the spectrum of PI-ISO-RT. According to ¹³C-NMRspectra simulations of the PMDA/MDI dimer transition to pentamer, anupfield shift for the resonance of carbon number 16 as the polymerbecomes longer is expected, suggesting that PI-ISO-RT consists of longerpolymer chains than PI-AMN-190. The ¹³C-NMR spectrum of PI-ISO-90,(which was also prepared in NMP just like PI-AMN-190), is identical tothe spectrum of the latter, signifying the importance of the solventpolarity in the nucleation and growth mechanism by which the twomaterials are formed. FIG. 7 shows room temperature (20° C.) liquid¹³C-NMR in DMSO-d₆ of a PMDA/MDI mixture (1:1 mol:mol, 12% w/w solidsformulation). The bottom two spectra are of the monomers. Times reportedrefer to the time lapsed after mixing. The last spectrum at the topcorresponds to the point just before gelation. FIGS. 5a and 5b show peakassignment (by spectrum simulation).

Experimental Methods

Pyromellitic dianhydride (PMDA) (e.g., obtained from Chriskev Company,Inc.); 4,4′-diisocyanatodiphenylmethane (4,4′-methylene diphenyldiisocyanate, MDI); 4,4′-methylenedianiline (MDA); acetic anhydride((Ac)₂O) (e.g., obtained from Acros Chemicals); and pyridine (e.g.,obtained from Fisher Scientific) may be used. AnhydrousN-methyl-2-pyrrolidone (NMP), acetonitrile, dimethylsulfoxide (DMSO),and absolute ethanol were used (e.g., obtained from Aldrich ChemicalCo). Deuterated DMSO (DMSO-d₆) was also used (e.g., obtained fromCambridge Isotope Laboratories, Inc).

Preparation of polyimide aerogels via the anhydride/diamine route(PI-AMN) will now be described.

Pyromellitic dianhydride (15.696 g, 0.072 mol) and4,4′-methylenedianiline (14.256 g, 0.072 mol) were added in variableamounts of NMP in a 250-mL round bottom flask under magnetic stirring.For example, for the 15% w/w solids formulation (samples referred to asPI-AMN-15) the amount of NMP was 169.7 g. The solution was stirred atroom temperature under nitrogen for 12 h and the color changed fromcolorless to yellow. At that point, acetic anhydride (in 6.3 mol excessto pyromellitic dianhydride) and pyridine (1:1 mol ratio to aceticanhydride) were added to the resulting polyamic acid solution, and thenew solution (sol) was poured into molds and was allowed to gel at roomtemperature. As molds for samples used for general chemical and physicalcharacterization, Wheaton 4-mL Polypropylene Omni-Vials with a 1.04-cminner diameter were used (Fisher part No. 225402), and for samples usedfor mechanical testing 30-mL Fisherbrand Class B Amber Glass TreadedVials were used, 2.1-cm inner diameter (Fisher part No. 03-339-23E). Thegelation time depends on the formulation: for 2.5%, 5%, 10% and 20% w/wsolids (PMDA+MDA) in the original NMP solution the gelation time was ˜4h, ˜1.5 h, 15 min and <15 min, respectively. The gels were aged in themolds for 12 h; subsequently they were washed with NMP (3×, 8 h eachtime, using 4× the volume of the gel each time), cured at 190° C. for 3h in the last NMP wash solution, cooled to room temperature, washed withethanol (4×, 8 h each time, using 4× the volume of the gel for eachwash) and dried into polyimide aerogels in an autoclave with liquid CO₂,taken out at the end supercritically.

Preparation of polyimide aerogels via the isocyanate route (PI-ISO) atroom temperature and at 90° C. will now be described.

At room temperature, MDI (2.50 g, 0.01 mol) was added under stirring toa mixture of NMP and acetonitrile (3:1 w/w), or NMP and DMSO (1:1 w/w)in a three-neck round bottom flask under N₂ at room temperature. Oncethe isocyanate was dissolved, pyromellitic dianhydride (2.18 g, 0.01mol) was added. For example, for a 15% w/w solids formulation the amountof NMP and acetonitrile were 19.88 g (19.34 mL) and 6.62 g (8.43 mL),respectively. Similarly for a 10% w/w solids formulation, the amounts ofNMP and DMSO were 21.06 g and 21.06 g respectively. The reaction mixturewas stirred under nitrogen for 1 h. The resulting sol was poured inmolds (see above), which were allowed to stand at room temperature.Gelation takes usually 6 h-48 h depending on the formulation. Forexample, in NMP:CH₃CN (3:1 w/w), the 10%, 15%, 20% and 30% w/w solidsformulations take 2 days, 36 h, 18 h, and 12 h, respectively. Bycomparison, a 15% w/w solids formulation in NMP takes 48 h for gelationat RT. Gels were aged in the molds for 24 h-8 days depending on thegelation time, typically four times the gelation time. Subsequently,gels were removed from the molds and were initially washed(solvent-exchanged) with NMP:acetonitrile (3:1 v/v), then withNMP:acetonitrile:acetone (2:1:1 v/v/v), NMP:acetone (1:1 v/v), andfinally with pure acetone. Similarly, gels synthesized in NMP/DMSO wereplaced in pure NMP, the second wash was carried out with NMP:acetone(3:1 v/v) the third with NMP:acetone (1:1 v/v), and finally gels wereplaced in pure acetone. After 4 acetone washes (8 h each time, using 4×the volume of the gel for each wash) wet gels were dried into polyimideaerogels in an autoclave with liquid CO₂, taken out at the endsupercritically.

At 90° C., a more time-efficient synthesis of PI-ISO was carried out atslightly (by polyimide standards) elevated temperatures as follows:pyromellitic dianydride (2.18 g, 0.01 mol) and MDI (2.50 g, 0.01 mol)were added in variable amounts of NMP in a three-neck round bottom flaskunder nitrogen at room temperature. For example, for a 15% w/w solidsformulation the amount of NMP was 26.52 g. The flask was placed in a 60°C. bath and the solution was stirred under N₂ for 0.5 h. The resultingsol was poured into molds (see above), which were heated in an ovensuccessively at 60° C., 70° C. and 80° C. for 3 h at each temperature.Although gelation of the PMDA/MDI/NMP mixture may occur even at roomtemperature over longer periods of time as described above, according tothis protocol, gelation usually occurs at the early stages of the 60° C.heating. Gels were first aged at 90° C. for 12 h in their molds, andsubsequently they were removed from the molds and placed directly infresh ethanol. After four ethanol washes (8 h each time, using 4× thevolume of the gel for each wash) wet gels were dried into polyimideaerogels in an autoclave with liquid CO₂, taken out at the endsupercritically.

Conversion of polyimide aerogels into carbon aerogels will also bedescribed.

PI-AMN and PI-ISO aerogels were pyrolyzed at 800° C. for 3 h in a tubefurnace under a flowing stream of Ar. Before heating, the tube waspurged with Ar for 10 min, and the heating rate was set at 5° C. min⁻¹.At the end of the heating period, the power to the furnace wasdisconnected and the tube was allowed to cool slowly back to roomtemperature under flowing Ar.

Carbon aerogels were etched by placing the aerogels in a tube furnaceunder flowing argon and were heated at 1000° C. The flowing gas wasswitched to CO₂ and the temperature was maintained at that level for 3h. Subsequently the flowing gas was switched back to Ar and the power tothe furnace was disconnected, allowing for slow cooling back to roomtemperature.

Drying with supercritical fluid CO₂ was conducted in an autoclave(SPI-DRY Jumbo Supercritical Point Dryer, SPI Supplies, Inc. WestChester, Pa.). Aerogel bulk densities (ρ_(b)) were calculated from theweight and physical dimension of the samples. Skeletal densities (ρ_(s))were determined with helium pycnometry using a Micromeritics AccuPyc II1340 instrument. Porosities, H, were determined from ρ_(b) and ρ_(s)according to: Π=100×[(1/ρ_(b))−(1/ρ_(s))]/(1/ρ_(b)). BET surface areas(σ) and pore size distributions were measured with nitrogenadsorption/desorption porosimetry using a Micromeritics ASAP 2020Surface Area and Porosity Analyzer. Samples for surface area andskeletal density determination were outgassed for 24 h at 80° C. undervacuum before analysis. Average pore diameters were determined by the4×V_(Total)/σ method, where V_(Total) is the total pore volume per gramof sample. V_(Total) is calculated either from the single highest volumeof N₂ adsorbed along the adsorption isotherm or from the relationshipV_(Total)=(1/ρ_(b))−(1/ρ_(s)). The single point N₂ adsorption methodtends to underestimate V_(Total) significantly when macropores areinvolved, and thus numerical proximity of the values determined by thetwo methods is used as a semi-quantitative criterion for evaluatingmacroporosity. Scanning electron microscopy (SEM) was conducted using aHitachi S-4700 Field Emission instrument. Chemical characterization ofall polyimide aerogels was based on IR and solid state ¹³C NMR. Infraredspectra were obtained in KBr pellets using a Nicolet-FTIR model 750Spectrometer. Solid-state ¹³C NMR spectra were obtained with samplesground in fine powders on a Bruker Avance 300 spectrometer (75.475 MHzcarbon frequency), using magic angle spinning (5 kHz) with broadbandproton suppression and the CPMAS TOSS pulse sequence for spin sidebandsuppression. ¹³C NMR spectra were externally referenced to the carbonylof glycine (176.03 ppm relative to tetramethylsilane). ¹³C-NMR peakassignment was aided by NMR spectra simulations using ChemDraw Ultra7.0. Thermogravimetric analysis (TGA) was conducted under nitrogen witha TA Instrument, model Hi-Res-TGA 2950 using ˜10 mg samples and aheating rate of 10° C. min⁻¹. The reaction between PMDA and MDI wasmonitored in DMSO-d₆ at room temperature up to the gelation point byliquid ¹³C NMR using a 400 MHz Varian Unity Inova NMR instrument. Thecrystallinity of the polyimide samples was determined by x-raydiffraction (XRD) using a Scintag 2000 diffractometer with Cu Kαradiation and a proportional counter detector equipped with a flatgraphite monochromator. The identity of the fundamental building blocksof the two materials was probed with small angle neutron scattering(SANS) using ˜2 mm thick discs cut with a diamond saw from cylinders, ona time-of-flight, low-Q diffractometer, LQD, at the Manuel Lujan Jr.Scattering Center of the Los Alamos National Laboratory. The scatteringdata are reported in the absolute units of differential cross sectionper unit volume (cm⁻¹) as a function of Q, the momentum transferredduring a scattering event. Quasi-static mechanical testing undercompression was conducted on an Instron 4469 universal testing machineframe, following the testing procedures and specimen length/diameterratio (equal to one) in ASTM D1621-04a (Standard Test Method forCompressive Properties of Rigid Cellular Plastics). The recorded forceas a function of displacement (machine-compliance corrected) wasconverted into stress as a function of strain. Four-point-probeconductivity measurements were conducted on flat surface of rectangularblock of carbon aerogel samples (made with a fine sand paper) using anAlesis contact probe station model CPS-06 with a Cascade Microtechelectrode model C4S-44/55. The reliability of the probe was confirmedwith silicon wafers and indium-tin-oxide coated glass slides of knownsheet resistance.

Macroscopic Characterization of PI-ISO Versus PI-AMN

General materials properties of polyimide aerogels synthesized bymethods shown in FIGS. 2a and 2b are summarized in Table 1. FIG. 8 showsphotographs of polyimide aerogels synthesized with 15% solids undervarious conditions also summarized in Table 1. Despite that sols areformulated based on weight percent of solids in solvents of differentdensities, attention was paid so that the molar monomer concentrationsin the different sols, ([C], see Table 1), remained about equal,allowing for a direct comparison. PI-AMN aerogels appear mechanicallystronger than the corresponding PI-ISO, but as mentioned above they alsoshrink significantly with respect to their molds (from 42% at the lowestgelation limit of 2.5% w/w solids, to 25% at the maximum solubilitylimit of 20% w/w solids). On the other hand, PI-ISO samples are alsorobust but soft, and shrink significantly less than PI-AMN under anypreparation conditions—in some cases even less than 1%. Shrinkage isreflected upon the bulk densities (ρ_(b)) of the final aerogels. FIG. 11summarizes data for shrinkage in a linear dimension (e.g., the cylinderdiameter) of samples of Table 1. PI-AMN samples shrink much more thanPI-ISO prepared using similar monomer concentrations (see Table 1). Atsimilar solids concentration formulations, the density of the PI-ISOsamples is lower than that of the PI-AMN samples (e.g., at 20% w/wsolids formulation, which is the highest solubility recorded of PI-AMN,the density of the PI-ISO samples is 0.2 g cm⁻³ versus 0.3 g cm⁻³ forthe PI-AMN samples). Further, the lowest ρ_(b) values with PI-AMNattainable are ˜0.09 g cm⁻³, while easy-to-handle PI-ISO monoliths withρ_(b) as low as 0.05 g cm⁻³ are readily prepared.

TABLE 1 Materials characterization data for polyimide aerogels Same Name(Composition- Process- Bulk Skeletal Temperature-% Linear Density,Density, Crystallinity w/w Solids)^(a) [C], M Shrinkage (%)^(e) ρ_(b) (gcm⁻³) ρ_(s) (g cm⁻³)^(g) (%) [°2θ] PI -AMN-190-2.5^(d) 5.78 × 10⁻⁵ 41.60.090 1.547 ± 0.104 45 [21, 29] PI-ISO-RT -2.5^(c,d) 5.14 × 10⁻⁵ 35.3 f1.595 ± 0.102 f PI-AMN-190-5 1.17 × 10⁻⁴ 38.0 ± 0.1^(j)  0.142 ±0.021^(j)  1.478 ± 0.045 37 [21, 28] PI-ISO-RT-5^(b) 1.18 × 10⁻⁴  5.0 f1.526 ± 0.045 42 [19, 25] PI-ISO-RT-5^(c) 1.04 × 10⁻⁴ 18.87 ± 0.02^(j) 0.047 ± 0.002^(j)  1.534 ± 0.080 37 [18]    PI-AMN-190-10 2.37 × 10⁻⁴30.04 ± 0.02^(k) 0.186 ± 0.016^(k) 1.453 ± 0.015    41 [21, 29, 42]PI-ISO-RT-10^(b,k) 2.33 × 10⁻⁴  2.1 ± 0.9^(k) 0.112 ± 0.003^(k) 1.490 ±0.023 23 [18]    PI-ISO-RT-10^(c,k) 2.11 × 10⁻⁴ 10.03 ± 0.03^(k) 0.090 ±0.006^(k) 1.473 ± 0.022 59 [43, 49] PI-AMN-190-15 3.61 × 10⁻⁴ 28.24 ±0.01^(k) 0.232 ± 0.008^(k) 1.474 ± 0.024 35 [22, 26] PI-AMN-RT-15 3.61 ×10⁻⁴ 35.0 ± 0.3^(k) 0.376 ± 0.006^(k) 1.432 ± 0.018 37 [35, 48]PI-ISO-90- 15 3.43 × 10⁻⁴ 17.48 ± 0.02^(k) 0.223 ± 0.014^(k) 1.551 ±0.037    33 [22, 27, 44] PI-ISO-RT -15^(b) 3.54 × 10⁻⁴  <1.0^(k) 0.167 ±0.002^(k) 1.447 ± 0.021 17 [17]    PI-ISO-RT-15^(c) 3.22 × 10⁻⁴  3.19 ±0.01^(k) 0.124 ± 0.001^(k) 1.398 ± 0.009 42 [43, 49] PI-AMN-190-20 4.89× 10⁻⁴ 24.89 ± 0.02^(k) 0.291 ± 0.022^(k) 1.437 ± 0.016 31 [21, 29]PI-ISO-90 -20 4.64 × 10⁻⁴  5.87 ± 0.01^(k) 0.266 ± 0.011^(k) 1.454 ±0.009 33 [18]    PI-ISO-RT-20^(b) 4.77 × 10⁻⁴  2.78 ± 0.03^(k) 0.208 ±0.001^(k) 1.415 ± 0.022 22 [18]    PI-ISO-RT-20^(c) 4.36 × 10⁻⁴  1.27 ±0.01^(k) 0.196 ± 0.001^(k) 1.461 ± 0.014 31 [17, 19] PI-ISO-90 -30 7.17× 10⁻⁴   4.71 ± 0.001^(l) 0.382 ± 0.003^(l)  1.473 ± 0.031 31 [17]   PI-ISO-RT-30^(c) 6.78 × 10⁻⁴  <1.0^(l) 0.285 ± 0.027^(l)  1.445 ± 0.00933 [17, 20] PI-ISO-90-40 9.84 × 10⁻⁴   4.90 ± 0.001^(l) 0.513 ±0.011^(l)  1.432 ± 0.009 32 [17, 19] PI-ISO-RT-40^(c) 9.36 × 10⁻⁴  3.8 ±0.2^(l) 0.417 ± 0.008^(l)  1.443 ± 0.007 42 [27, 43] PI-ISO-90-50 1.27 ×10⁻³   5.50 ± 0.00₃ ^(l) 0.679 ± 0.002^(l)  1.452 ± 0.014 33 [19, 25]Same Name (Composition- BET Average Average Process- Porosity, SurfacePore Pore Temperature-% Π (% void Area, Diameter Diameter w/wSolids)^(a) space) σ(m² g⁻¹) (nm)^(h) (nm)^(i) PI -AMN-190-2.5^(d) 94385  17.0 [108.5] 42.7 [60.4] PI-ISO-RT -2.5^(c,d) f 297 14.7 [f]   35.5 [55.0] PI-AMN-190-5 90 412 29.6 [62.0] 47.0 [11.4] PI-ISO-RT-5^(b)f 374 13.8 [f]    36.3 [67.3] PI-ISO-RT-5^(c) 97 333  23.0 [250.4] 36.3[45.7] PI-AMN-190-10 87 431 29.5 [45.8] 40.7 [22.1] PI-ISO-RT-10^(b,k)93 373 28.9 [88.9] 41.7 [37.1] PI-ISO-RT-10^(c,k) 94 316  25.6 [131.6]39.8 [38.4] PI-AMN-190-15 84 413 26.5 [35.3] 31.6 [17.1] PI-AMN-RT-15 74299 11.2 [26.2] 14.5 [9.4]  PI-ISO-90- 15 85 244 14.2 [62.6] 39.8 [66.6]PI-ISO-RT -15^(b) 88 391 25.5 [54.3] 31.6 [28.4] PI-ISO-RT-15^(c) 91 31533.5 [93.2] 52.5 [34.3] PI-AMN-190-20 80 378 18.2 [29.0] 24.0 [11.9]PI-ISO-90 -20 80 246 20.0 [50.0] 24.0 [11.8] PI-ISO-RT-20^(b) 85 36623.0 [44.7] 30.9 [30.8] PI-ISO-RT-20^(c) 87 352 22.7 [84.7] 39.8 [26.1]PI-ISO-90 -30 74 303 13.2 [51.2] 24.5 [30.0] PI-ISO-RT-30^(c) 80 33922.4 [33.3] 40.7 [32.2] PI-ISO-90-40 64 278 10.7 [17.8] 14.1 [25.6]PI-ISO-RT-40^(c) 71 171 12.0 [39.7] 39.8 [40.2] PI-ISO-90-50 53 222  6.3[14.1] 8.5 [7.2] ^(a)PI-AMN: Polyimide samples synthesized through theamine route; PI-ISO: polyimide samples synthesized through theisocyanate route; PI-AMN-190: samples cured in NMP at 190° C. beforedrying; PI-AMN-RT: samples dried supercritically without further curingat 190° C.; PI-ISO-90: samples synthesized at 60-90° C. in NMP;PI-ISO-RT: samples synthesized at room temperature. ^(b)PI-ISO-RTsamples synthesized in NMP/DMSO. ^(c)PI-ISO-RT samples synthesized inNMP/acetonitrile). ^(d)Single sample. ^(e)Shrinkage = 100 × (molddiameter − sample diameter)/(mold diameter). f. Irregular shape, was notmeasured. ^(g)Single sample, average of 50 measurements. ^(h)By the 4 ×V_(Total)/σ method. For the first number, V_(Total) was calculated bythe single-point adsorption method; for the number in brackets,V_(Total) was calculated via V_(Total) = (1/ρ_(b)) − (1/ρ_(s)). ^(i)Fromthe BJH plots: The first numbers are the peak maxima; the numbers inbrackets are the width at half maxima of the BJH plots. ^(j)Average of 2samples. ^(k)Average of 4 samples. ^(l)Average of 3 samples.

Partly owing to the similar chemical composition of the two materials,partly to their similar degree of crystallinity (30-45% by XRD, seeTable 1), and partly to similar packing distances within the crystallinephases (expressed by similar 20 values, see Table 1), skeletaldensities, A, of all samples are in the 1.4-1.5 g cm⁻³ range, which iscomparable with the density of bulk polyimides obtained from PMDA andMDA (1.357 g cm⁻³). The similar ρ_(s) values but the different ρ_(b)'sare reflected in the porosities, which are higher for the PI-ISOaerogels relative to the corresponding PI-AMN samples. However, BETsurface areas, σ; from N₂-sorption data show an opposite trend from theporosities: despite higher shrinkage, higher bulk densities and lowerporosities, PI-AMN samples have about equal or higher surface areas thanPI-ISO samples. These data point to significant differences in thenanomorphology of the PI-AMN versus the PI-ISO samples, which arediscussed in the next section. FIG. 12 shows representative N₂-sorptiondata (insets showing BJH plots) of polyimide aerogels prepared using the15% w/w solids formulations (Table 1). FIG. 12(A) depicts PI-AMN-190(ρ_(b)=0.23 g cm⁻³); and FIG. 12(B) shows PI-ISO-RT prepared in NMP/DMSO1:1 w/w (ρ_(b)=0.17 g cm⁻³).

Structural Characterization of PI-ISO Versus PI-AMN

The microstructure of polyimide aerogels was evaluated in terms of theirpore-size distribution and the nanomorphology of their skeletalframeworks. The pore-size distribution at the meso/macro scale wasevaluated semi-quantitatively by analysis of the N₂-sorption data incombination with SEM, while the elementary building blocks of theskeletal framework were probed with SANS. Data shown concern samplesobtained with the 15% w/w solids formulation. Similar data and trendshave been observed with samples prepared with all other solidsformulations (Table 1).

For both PI-AMN and PI-ISO samples, N₂-sorption isotherms show a rapidincrease of the volume adsorbed at relative pressures above 0.9, whichin combination with the narrow desorption loop indicates the presence ofboth meso- and macroporosity. Indeed, pore size analysis via therelationship (pore diameter)=4×V_(Total)/σ, where V_(Total) iscalculated either from the maximum adsorption point in the isotherm, orthe relationship V_(Total)=(1/ρ_(b))−(1/ρ_(s)), gives quite differentvalues (Table 1), which get progressively closer as the bulk densityincreases, as expected by the fact that more dense materials should havesmaller pores. The BJH-desorption method reflects the mesoporosity andyields pore diameters closer to those obtained by the single pointabsorption method (Table 1), but it also shows quite broad pore sizedistributions (evaluated by the width at half maxima of the BJH plots,see Table 1). Overall, the N₂-sorption method indicates that both PI-AMNand PI-ISO aerogels are meso/macroporous materials. SEM, however, showsthat their pore structures are quite different: at all densities PI-AMNare particulate while PI-ISO are fibrous. At high magnifications, therewas a discernible primary/secondary particle structural hierarchy in thecase of PI-AMN, while in some cases it can be also claimed that thePI-ISO ribbons consist of particles. FIG. 13 illustrates SEM data at twodifferent magnifications of polyimide aerogels prepared using the 15%w/w solids formulations (Table 1). FIG. 13(A) shows PI-AMN-190(ρ_(b)=0.23 g cm⁻³); and FIG. 13(B) shows PI-ISO-RT prepared inNMP/CH₃CN 3:1 w/w (ρ_(b)=0.12 g cm⁻³). FIG. 14 shows SEM data of (A)PI-AMN (ρ_(b)=0.186 g/cm³, porosity=87%, ρ_(s)=1.456 g/cm³, BET surfacearea=431 m²/g); and (B) PI-ISO (ρ_(b)=0.090 g/cm³, porosity=94%,ρ_(s)=1.473 g/cm³, BET surface area=315 m²/g).

The make-up of the skeletal frameworks in PI-AMN and PI-ISO was probedquantitatively with SANS. To exclude the effect of the solvent, whichcontrols phase-separation, and therefore affects the size of theparticles, the specific materials compared were both prepared in NMP(PI-ISO-90 and PI-AMN-190). While scattering from PI-AMN and PI-ISO isdistinct, there are similarities. To facilitate analysis, and as shownin FIG. 15, scattering has been broken down into four regions. Eachmaterial displays two length-scales (regions I and III) and twopower-law regions (linear sections on a log-log plot, regions II andIV). In region IV both materials display power-law scattering withexponents of ˜5 (PI-ISO: 5.0±0.1; PI-AMN: 5.1±0.1). FIG. 15 shows SANSdata of PI-AMN-190 (black line, ρ_(b)=0.23 g cm³) and of PI-ISO-90 (redline, ρ_(b)=0.22 g cm⁻³) both prepared in NMP using the 15% w/w solidsformulation. Vertical lines separate the power-law regions (II and IV)from the “knee” regions (I and III). For smooth interfaces, the exponentin this region is typically 4, while for fractally-rough interfaces itis 3-4. Exponents >4 are largely attributed to rapidly changing densityat the interface. In region III, both materials display a “knee,” whichis indicative of a fundamental length-scale and may relate to smallpores, the cross section of a foam strut, or the primary particle sizeof aggregates forming the material. The first two possibilities areexcluded based on the similar skeletal densities of the two materials(absence of small pores) and the quite different SEM microstructures(different cross-sections of the skeletal frameworks). Region III kneesare attributed to the primary particles forming the materials. Analysisaccording to the Unified Model provides the radius of gyration (R_(g)),where for spherical particles R_(g)≈0.77R (R is the average radius ofthe particles). For PI-AMN, R_(g)=5.8 nm and for PI-ISO, R_(g)=4.7 nm.In region II, both materials exhibit power-law scattering again. PI-AMNexhibits a power-law with an exponent of ˜2 and PI-ISO exhibits anexponent of ˜1. For fractal systems, an exponent of 2 would indicatepore (or mass) fractals, while for simple shapes it is indicative of asheet- or disk-like morphology; an exponent of 1 is indicative of acylindrical-like morphology, which would describe the fibers of PI-ISO.Finally, in region I both materials display “knees,” which may againrelate to larger pores, the cross section of a foam strut or the size ofan aggregate of particles. For PI-AMN, R_(g)=35 nm and for PI-ISO,R_(g)=41.6 nm. Based on SEM, in the case of PI-AMN those structuralelements are attributed to secondary particles and in the case of PI-ISOto the diameter of the fibers. It is noted that length-scales identifiedby SANS agree well with feature sizes seen at the higher magnificationSEM.

Overall, chemically identical (case of PI-AMN-190 and PI-ISO-90) andstructurally very similar primary particles (in terms of crystallinityand size) seem to form secondary particles in the case of PI-AMN, andfibers in the case of PI-ISO. The size of the primary particles may becontrolled by the common solvent (NMP). Then, the variable that remainsdifferent in the two systems is the actual chemistry of the twoprocesses, which is translated into the surface functionality of theprimary particles. It is suggested that the flexible amic acid bridgesbetween PI-AMN primary particles allows pivoting, closer packing, and a3D growth resulting into secondary particles; on the other hand, therigidity of the seven-member ring between PI-ISO primary particles, incombination with steric hindrance from neighboring particles, imposesgrowth at the exposed ends of the assembly resulting in directionalgrowth and fibers. FIGS. 6a and 6b illustrate a molecular schematic ofthe interfacial chemistry of primary particles in PI-AMN and PI-ISO.

The 3D growth in PI-AMN creates numerous crosslinks between secondaryparticles while in the case of PI-ISO, crosslinking may take place onlyat the contacts between fibers. This model for PI-AMN versus PI-ISOaerogels is supported by the higher shrinkage of PI-AMN, and may serveas an explanation for their high compressive mechanical strength, whichcompares favorably with that of structurally analogous polymercrosslinked silica aerogels at the same densities. On the other hand, atsimilar percent solids formulations, PI-ISO aerogel monoliths aremechanically much weaker materials, undergoing premature catastrophicfailure to large pieces with much smaller loads. In some embodiments,entangled nanofibrous structures are generally mechanically stronger(the bird-nest effect).

FIG. 16 depicts behavior under compression (ASTM D1621-04a) of aPI-AMN-190 sample prepared using the 20% w/w solids formulation (Table1): a short linear elastic range (at <(1.175±0.075)% strain, magnifiedand shown as an inset) is followed by plastic deformation (up to 50%strain) and inelastic hardening thereafter. The samples did not failunder compression. Other data pertinent to mechanical characterization(averages of two samples): bulk density ρ_(b)=0.291±0.006 g cm³; maximumstrength (at 86% engineering strain): 99.27±3.64 MPa; specific energy atmaximum load (at 86% engineering strain): 48.04±2.48 J g⁻¹; Young'smodulus (from the slope of the linear elastic range in the inset):27.25±0.84 MPa; yield strength (stress at 0.2% offset strain):1.525±0.388 MPa (calculated by drawing a parallel line to the slope ofthe linear elastic range in the inset, starting from engineeringstrain=0.002); yield stain (i.e., strain at yield strength): 3.10±0.45;linear elastic to total deformation at the yield point: 0.38.

Pyrolysis of Polyimide Aerogels and Conversion to Carbon

Porous carbons are pursued as electrodes for fuel cells and batteries.Polyimides generally have good carbonization yields, and in fact thefirst PI-AMN aerogels reported were also investigated for theirconversion to carbon aerogels (pyrolytically) and metal carbide aerogels(carbothermally, after doping with selected sol-gel-derived metaloxides). Carbonizable polymers are capable of either cyclizing, orundergoing ring fusion and chain coalescence by heating. For this thechain should either contain aromatic moieties or be aromatizable(usually by oxidation). In the former case, there is one carbon atombetween aromatic rings; otherwise, pyrolytic chain scission will prevailleading to loss of fragments. The PMDA/MDI or MDA polyimides hereinfulfill the last criterion. By thermogravimetric analysis under N₂ (TGA)both PI-AMN and PI-ISO are stable up to about 550° C., subsequentlyloosing 40-50% of their mass before 650° C. (presumably by loss of smallmolecules like CO and CO₂). FIG. 17 shows comparative TGA data forsamples indicated prepared using 15% w/w solids formulations. Theadditional gradual mass loss at higher temperatures is attributed toloss of nitrogen-containing fragments. Carbonization pyrolysis wascarried out at 800° C. under Ar for 3 h. Pertinent data concerning theresulting carbon aerogels are summarized in Table 2 for various samplesprepared with the 15% w/w and the 10% w/w solids formulations (forcomparison, refer to Table 1).

TABLE 2 Properties of PI-AMN and PI-ISO derived carbon aerogels^(a)Precursor for Pyrolytic Carbonization BET (Sample- Carbon Linear BulkSkeletal Surface Additional Yield % Shrinkage Density, Density,Porosity, Area, Processing) (w/w) (%)^(g) ρ_(b) (g cm⁻³) ρ_(s) (gcm⁻³)^(j) Π (% v/v) σ(m² g⁻¹) PI-AMN-190-15 58 ± 2^(e) 48.0 ± 0.5 [63]1.018 ± 0.153^(h) 1.896 ± 0.070 46 113 PI-ISO-90-15 55 ± 2^(e) 40.8 ±0.4 [52] 0.665 ± 0.064^(h) 1.998 ± 0.057 67 279 PI-ISO-RT-10^(b) 53 ±2^(e) 61.6 ± 0.9 [64] 1.012 ± 0.117^(i) 1.863 ± 0.034 46 336PI-ISO-RT-10^(c) 53.6 ± 0.4^(e)    62 ± 2 [66] 0.967 ± 0.160^(i) 1.729 ±0.021 44 361 PI-AMN-190-15 79^(f)       3 [63] 0.701 2.114 ± 0.069 67417 3 h-CO₂ ^(d) PI-ISO-RT-10 59^(f)     8.7 [65] 0.670 2.310 ± 0.052 711010 3h-CO₂ ^(b, d) ^(a)PI-AMN and PI-ISO samples as indicated,processed at 800° C. under Ar for 3 h. ^(b)PI-ISO-RT samples synthesizedat in NMP/DMSO. ^(c)PI-ISO-RT samples synthesized in NMP/acetonitrile.^(d)Resulting carbon samples processed for an additional 3 h at 1000° C.under flowing CO₂. ^(e)Average of four samples. ^(f)Single sample; yieldrelative to the sample before treatment with CO₂ at 800° C. for 3 h.^(g)Shrinkage = 100 × (sample diameter before pyrolysis − samplediameter after pyrolysis)/(sample diameter before pyrolysis); for thenumber in the brackets, shrinkage was calculated with respect to theoriginal mold diameter. ^(h)Average of two samples. ^(i)Average of 3samples. ^(j)Single sample, average of 50 measurements.

Polyimide aerogels remain as quite sturdy monoliths after pyrolysis.Carbon aerogels are also black in color. PI-AMN-derived carbons,however, have a metallic luster, while PI-ISO derived samples are dull.The carbonization yield generally is between 51-56% w/w. Carbon aerogelsshrink further beyond their initial imidization shrinkage (Table 1), butPI-ISO-RT samples shrink more (˜60%) than the PI-AMN samples (˜50%), sothat the total shrinkage calculated from the initial molds (Table 2) isapproximately the same for both kinds of samples (63-66%). The PI-ISO-90samples seem to have a small advantage over the rest in terms ofshrinkage (overall 52% relative to the molds).

Chemically, pyrolytic samples consist only of carbon (as determined byEDS). XRD shows very broad diffractions. Typical Raman spectra show boththe G (graphitic) and D (disordered) peaks at 1352 cm⁻¹ and 1597 cm⁻¹,respectively. FIG. 18 shows Raman spectra of polyimide aerogels preparedby the two routes. The ratios of the integrated peak intensities(I_(D)/I_(G)) are 1.12 and 0.98 for carbon aerogels obtained from PI-ISOand PI-AMN, respectively, indicating that all carbons arenanocrystalline/amorphous. Indeed, the skeletal densities of all samplesare in the 1.7-2.0 g cm⁻³ range (Table 2), which is what is expectedfrom amorphous carbon (1.8-2.0 g cm³). Combination of bulk and skeletaldensities yields porosities in the range of ˜45% v/v of empty space,which are significantly lower than the porosities of the parentpolyimide aerogels (compare Tables 1 and 2). An exception is thePI-ISO-90 samples where the porosity is 67% v/v of empty space and isattributed to their lower pyrolytic shrinkage (Table 2).

Microscopically (by SEM) PI-AMN-derived carbons are different from theirparent polyimide aerogels. FIG. 19 shows SEM at two differentmagnifications and N₂-sorption data for carbon aerogels produced bypyrolysis at 800° C. under nitrogen. FIG. 19(A) shows PI-AMN-190prepared by the 15% w/w solids formulation in NMP; and FIG. 19(B) showsPI-ISO-RT prepared by the 10% w/w solids formulation in NMP/CH₃CN 3:1w/w. FIG. 20 shows SEM data (scale bars at 200 nm) and N₂-sorption datafor carbon aerogels after etching at 1000° C. under flowing CO₂ for 3 h.FIG. 20(A) shows carbon aerogel from PI-AMN-190 prepared by the 15% w/wsolids formulation in NMP; and FIG. 20(B) shows carbon aerogel fromPI-ISO-RT prepared by the 10% w/w solids formulation in NMP/DMSO 1:1w/w. There is a notable rapid rise of the volume adsorbed at lowrelative pressures, indicating microporosity (pore sizes <2 nm). Thestructure is dominated by large macropores surrounded by “solid” walls,although N₂-sorption isotherms show the presence of all three kind ofpores: microporores (significant quick rise of the volume adsorbed atlow partial pressures), mesopores (presence of a hysteresis loop), andmacropores (second quick rise of the volume adsorbed above P/P_(o)˜0.9).The lower BET surface area relative to that of PI-AMN samples beforepyrolysis (113 m² g⁻¹ versus 413 m² g⁻¹, respectively) is consistentwith the changes observed by SEM. On the other hand, PI-ISO-derivedcarbons retain the fibrous nanomorphology of the parent polyimideaerogels, but the fine structure that could be seen on the fibers of theparent PI-ISO aerogels has been erased. Again, N₂-sorption isothermsindicate the presence of all three kinds of pores, while the BET surfacearea of the PI-ISO-derived carbon aerogels has been increased somewhatrelative to that of the parent polyimides (compare Tables 1 and 2). Thispyrolytic behavior of both PI-AMN and PI-ISO samples is consistent withthe model of FIGS. 6a and 6b : at the early stages of pyrolysis bondbreaking and reforming at the surfaces of the primary and secondaryparticles (case of PI-AMN), leads to rearrangement and a more compactstructure. Macroscopically, that mechanism is expected to lead toshrinkage, and microscopically into large voids defined by compact walls(case of PI-AMN). On the other hand, in the case of PI-ISO bond breakingand reforming leads to smoother thinner fibers, but the pore structureis retained.

The presence of micropores indicated by the N₂-sorption isothermssuggests that a significant gain in surface area could be achieved byetching. That was carried out under flowing CO₂ at 1000° C. (carbon andCO₂ comproportionate to CO.) The results are included in Table 2.CO₂-treated samples lose 20-40% of their mass, shrink 3-9% and remainmonolithic. Consequently, bulk densities decrease, however, skeletaldensities increase to the 2.1-2.3 g cm⁻³ range (density of graphite at2.26 g cm³). The porosity is dominated by the bulk density decrease,reaching up to ˜70% v/v of empty space. Microscopically, PI-ISO samplesremain fibrous, while PI-AMN samples show macropores similar in shape tothose observed before etching. The number of those macropores hasincreased and surrounding walls seem rougher; considering these datatogether suggests that before etching many pores are masked by a thinporous crust of carbon. After CO₂-etching, the N₂-sorption isothermsindicate that the majority of the empty space is attributed tomicropores, while the BET surface areas of the samples increasesdramatically, reaching the levels of the parent polyimide aerogels inthe case of PI-AMN-derived carbons (417 m² g⁻¹), or far surpassing thoselevels in the case of PI-ISO-derived samples (1010 m² g⁻¹). For reasonsnot well understood yet, despite the mass loss CO₂-etching increases theelectrical conductivity of PI-ISO-derived carbon aerogels by ˜70×, from0.013 mho cm⁻¹ (at ρ_(b)=0.967 g cm⁻³) to 8.697 mho cm⁻¹ (at ρ_(b)=0.670g cm³). (By comparison the electrical conductivity of CO₂-etchedPI-AMN-derived carbon aerogels is 4.491 mho cm⁻¹ at ρ_(b)=0.701 g cm³.)Those values render polyimide-derived carbon aerogels particularlyattractive as electrochemical electrodes.

Three-dimensional porous polyimide and carbon networks derivedtherefrom, such as polyimide and carbon aerogels, are high value-addedmaterials and may be useful for a number of applications. For example,such porous polyimide networks may be useful in high-temperature thermalinsulation (e.g., architectural, automotive industrial applications,aircraft, spacecraft, clothing), lightweight structures, acousticinsulation (e.g., buildings, automobiles, aircrafts), impact dampening,dielectrics (e.g., for fast electronics), supports for catalysts, and ashosts of functional reactants for chemical, electronic and opticalapplications. In some embodiments, three-dimensional porous networksdescribed may be used as insulation material for apparel, such asclothing, astronaut suits, and armor.

Described herein are three-dimensional porous polyimide networkssynthesized via a low temperature process through a reaction ofdianhydrides with diisocyanates. Although MDI has been used, othermonomers such as 4,4′-oxybis(phenylisocyanate) may behave similarly andresulting polyimides may have the chemical composition of Kapton.Three-dimensional porous polyimide networks (e.g., polyimide aerogels)derived from PMDA/MDI may exhibit fibrous morphologies and can beconverted pyrolytically to isomorphic three-dimensional porous carbonnetworks (e.g., carbon aerogels), which, owing to their large surfacearea, may be useful for their reactivity with nanoparticulate oxidizingagents.

Three-dimensional porous polyimide networks including polyimide aerogelsmay be useful in applications that involve, for example, absorption ofoil or other hydrophobic materials. In some instances, such materialsmay be capable of absorbing 5, 15, 20, 25, or more times their weight inoil or other hydrophobic material. In some instances, the majority ofthe substance absorbed may be retrieved by chemical and/or mechanicalmethods. Three-dimensional porous carbon networks derived fromthree-dimensional porous polyimide networks may also be useful for anumber of applications including, for example, manufacture ofelectrodes, batteries, supercapacitors, high-temperature insulators,high-temperature ballistics materials, ablative materials and infraredblocking armor. In some embodiments, doping PI-ISO with cerium oxide andpyrolysis to carbon under argon may lead to materials that are selfignited when exposed to air, giving rise to potential energeticmaterials applications.

Having thus described several aspects of at least one embodiment of thisinvention, it is to be appreciated various alterations, modifications,and improvements will readily occur to those skilled in the art. Suchalterations, modification, and improvements are intended to be part ofthis disclosure, and are intended to be within the spirit and scope ofthe invention. Accordingly, the foregoing description and drawings areby way of example only.

What is claimed is: 1-19. (canceled)
 20. A polyimide aerogel comprisingthe following moiety:


21. A carbon aerogel derived from the polyimide aerogel of claim
 20. 22.The carbon aerogel of claim 21, wherein the carbon aerogel comprisesmicroporosity originating from chemical etching.
 23. A polyimide aerogelcomprising the following moiety:


24. A carbon aerogel derived from the polyimide aerogel of claim
 23. 25.The carbon aerogel of claim 24, wherein the carbon aerogel comprisesmicroporosity originating from chemical etching.
 26. A polyimide aerogelcomprising the following moiety:

wherein R originates from a triisocyanate.
 27. A carbon aerogel derivedfrom the polyimide aerogel of claim
 26. 28. The carbon aerogel of claim27, wherein the carbon aerogel comprises microporosity originating fromchemical etching.